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成人急性淋巴细胞白血病体外泼尼松龙耐药的生物学及临床意义

Biological and clinical significance of in vitro prednisolone resistance in adult acute lymphoblastic leukaemia.

作者信息

Tosi P, Visani G, Ottaviani E, Manfroi S, Tura S

机构信息

Institute of Haematology, Le A. Seràgnoli, University of Bologna, Italy.

出版信息

Eur J Haematol. 1996 Aug;57(2):134-41. doi: 10.1111/j.1600-0609.1996.tb01351.x.

Abstract

It has been reported that in vitro prednisolone (PDN) resistance provides a prognostic value in childhood acute lymphoblastic leukaemia (ALL). This study aimed at investigating the biological and clinical significance of in vitro PDN resistance in adult ALL. Blast cells from 30 patients were exposed to PDN (0.1 microM-35 microM) and cytotoxicity was determined by the soluble tetrazolium formazan 2,3-bis (2-methoxy-4-nitro-5-sulphophenyl)-5-[(phenylamino) carbamyl]-2H-tetrazolium hydroxyde (XTT) colorimetric assay. The IC50 (defined as the drug concentration that results in 50% growth inhibition) varied greatly among the samples, from 0.3 microM to > 35 microM; 15 microM was subsequently chosen as IC50-cut-off point between in vitro resistant and sensitive cases. PDN-induced cytotoxicity was significantly related to apoptosis, as demonstrated by regression analysis; in sensitive cases, however, the percentage of apoptotic cells after in vitro PDN treatment was significantly increased compared with control (p = 0.002). Immunofluorescence evaluation of intracellular BCL-2 protein showed an equal percentage of positive cells in the two groups, but in resistant cells a higher mean fluorescence intensity (p = 0.04) was demonstrated. In vitro sensitive and resistant patients did not display differences in clinical characteristics, in cytological, karyotypic and immunophenotypic features and in the outcome of induction therapy. Disease-free survival (DFS), however, was significantly better in sensitive patients (p = 0.02).

摘要

据报道,体外泼尼松龙(PDN)耐药性对儿童急性淋巴细胞白血病(ALL)具有预后价值。本研究旨在探讨体外PDN耐药性在成人ALL中的生物学和临床意义。对30例患者的原始细胞暴露于PDN(0.1微摩尔/升至35微摩尔/升),并通过可溶性四氮唑盐2,3-双(2-甲氧基-4-硝基-5-磺基苯基)-5-[(苯胺基)氨基甲酰]-2H-四氮唑氢氧化物(XTT)比色法测定细胞毒性。半数抑制浓度(IC50,定义为导致50%生长抑制的药物浓度)在样本中差异很大,从0.3微摩尔/升至>35微摩尔/升;随后选择15微摩尔/升作为体外耐药和敏感病例之间的IC50分界点。回归分析表明,PDN诱导的细胞毒性与细胞凋亡显著相关;然而,在敏感病例中,体外PDN处理后凋亡细胞的百分比与对照组相比显著增加(p = 0.002)。细胞内BCL-2蛋白的免疫荧光评估显示两组阳性细胞百分比相同,但耐药细胞中平均荧光强度更高(p = 0.04)。体外敏感和耐药患者在临床特征、细胞学、核型和免疫表型特征以及诱导治疗结果方面没有差异。然而,敏感患者的无病生存期(DFS)明显更好(p = 0.02)。

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